HIV inhibiting pyrimidine derivatives

ABSTRACT

This invention concerns the use of the compounds of formula  
                 
 
the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein A is CH, CR 4  or N; n is  0  to  4;  Q is hydrogen or —NR 1 R 2 ; R 1  and R 2  are selected from hydrogen, hydroxy, C 1-12 alkyl, C 1-12 alkyloxy, C 1-12 alkylcarbonyl, C 1-12 alkyloxycarbonyl, aryl, amino, mono- or di(C 1-12 alkyl)-amino, mono- or di(C 1-12 alkyl)aminocarbonyl wherein each C 1-12 alkyl may optionally be substituted: or R 1  and R 2  taken together may form pyrrolidinyl, piperidinyl, morpholinyl, azido or mono- or di(C 1-12 alkyl)aminoC 1-4 alkylidene; R 3  is hydrogen, aryl, C 1-6 alkylcarbonyl, optionally substituted C 1-6 alkyl, C 1-6 alkyloxy-carbonyl,; and R 4  is hydroxy, halo, optionally substituted C 1-6 alkyl, C 1-6 alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl, trihalomethyloxy; R 5  is hydrogen or C 1-4 alkyl; L is optionally substituted C 1-10 alkyl, C 3-10 alkenyl, C 3-10 alkynyl, C 3-7 cycloalkyl: or L is —X 1 —R 6  or —X 2 -Alk-R 7  wherein R 6  and R 7  are optionally substituted phenyl; X 1  and X 2  are —NR 3 —, —NH—NH—, —N═N—, —O—, —S—, —S(═O)— or —S(═O) 2 —; Alk is C 1-4 alkanediyl; aryl is potionally substituted phenyl; Het is an optionally substituted aliphatic or aromatic heterocyclic radical: for the manufacture of a medicine for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection. It further relates to new compounds being a subgroup of the compounds of formula (I), their preparation and compositions comprising them.

The present invention is concerned with pyrimidine derivatives having HIV replication inhibiting properties. The invention further relates to methods for their preparation and pharmaceutical compositions comprising them. The invention also relates to the use of said compounds in the manufacture of a medicament useful for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection.

Compounds structurally related to the present compounds are disclosed in the prior art.

JP-2,052,360, JP-2,308,248, JP-9,080,676 and JP-9,068,784 disclose a number of trisubstituted pyrimidines useful in photographic material. JP-8,199,163 discloses trisubstituted pyrimidines useful in an organic electroluminescent device. JP-2,300,264 and GB-1,477,349 disclose pyrimidinetriamines for their use in the dye industry.

J. Indian Chem. Soc. (1975), 52(8), 774-775 discloses the synthesis of some bis(arylamino)pyrimidines. J. Heterocycl. Chem. (1973), 10(2), 167-171 discloses the condensation of various aminopyrimidines with picryl halides. J. Org. Chem. (1961), 26, 4433-4440 discloses several triaminopyrimidines as intermediates in the synthesis of triazolo[4,5-d]pyrimidines.

WO 91/18887 discloses diaminopyrimidines as gastric acid secretion inhibitors.

Unexpectedly, it has now been found that the compounds of formula (I) effectively inhibit the replication of the Human Immunodeficiency Virus (HIV) and consequently may be useful for the treatment of individuals infected by HIV.

The present invention concerns the use of the compounds of formula

the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein

A is CH, CR⁴ or N;

n is 0, 1, 2, 3 or 4;

Q is hydrogen or —NR¹R²; R¹ and R² are each independently selected from hydrogen, hydroxy, C₁₋₁₂alkyl, C₁₋₁₂alkyloxy, C₁₋₁₂alkylcarbonyl, C₁₋₁₂alkyloxycarbonyl, aryl, amino, mono- or di(C₁₋₁₂alkyl)amino, mono- or di(C₁₋₁₂alkyl)aminocarbonyl wherein each of the aforementioned C₁₋₁₂alkyl groups may optionally and each individually be substituted with one or two substituents each independently selected from hydroxy, C₁₋₆alkyloxy, hydroxyC₁₋₆alkyloxy, carboxyl, C₁₋₆alkyloxycarbonyl, cyano, amino, imino, aminocarbonyl, aminocarbonylamino, mono- or di(C₁₋₆alkyl)amino, aryl and Het; or

R¹ and R² taken together may form pyrrolidinyl, piperidinyl, morpholinyl, azido or mono- or di(C₁₋₁₂alkyl)aminoC₁₋₄alkylidene:

R³ is hydrogen, aryl, C₁₋₆alkylcarbonyl, C₁₋₆alkyl, C₁₋₆alkyloxycarbonyl, C₁₋₆alkyl substituted with C₁₋₆alkyloxycarbonyl; and

each R⁴ independently is hydroxy, halo, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, amino-carbonyl, nitro, amino, trihalomethyl, trihalomethyloxy or C₁₋₆alkyl substituted with cyano or aminocarbonyl:

R⁵ is hydrogen or C₁₋₄alkyl;

L is C₁₋₁₀alkyl, C₃₋₁₀alkenyl, C₃₋₁₀alkynyl, C₃₋₇cycloalkyl, or C₁₋₁₀alkyl substituted with one or two substituents independently selected from C₃₋₇cycloalkyl, indanyl, indolyl and phenyl, wherein said phenyl, indanyl and indolyl may be substituted with one, two, three, four or where possible five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, aminocarbonyl, C₁₋₆alkyloxycarbonyl, formyl, nitro, amino, trihalomethyl, trihalomethyloxy and C₁₋₆alkylcarbonyl; or

L is —X¹—R⁶ or —X²-Alk-R⁷ wherein

R⁶ and R⁷ each independently are phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, C₁₋₆alkylcarbonyl, C₁₋₆alkyloxycarbonyl, formyl, cyano, aminocarbonyl, nitro, amino, trihalomethyloxy and trihalomethyl; and X¹ and X² are each independently —NR³—, —NH—NH—, —N═N—, —O—, —S—, —S(═O)— or —S(═O)₂—;

Alk is C₁₋₄alkanediyl;

aryl is phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, nitro and trifluoromethyl;

Het is an aliphatic or aromatic heterocyclic radical: said aliphatic heterocyclic radical is selected from pyrrolidinyl, piperidinyl, homopiperidinyl, piperazinyl, morpholinyl, tetrahydrofuranyl and tetrahydrothienyl wherein each of said aliphatic heterocyclic radical may optionally be substituted with an oxo group; and said aromatic hetero-cyclic radical is selected from pyrrolyl, furanyl, thienyl, pyridyl, pyrimidinyl, pyrazinyl and pyridazinyl wherein each of said aromatic heterocyclic radical may optionally be substituted with hydroxy;

for the manufacture of a medicine for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection.

The present invention also relates to a method of treating warm-blooded animals suffering from HIV (Human Immunodeficiency Virus) infection. Said method comprises the administration of a therapeutically effective amount of a compound of formula (I) or any subgroup thereof, a N-oxide form, a pharmaceutically acceptable addition salt or a stereochemically isomeric form thereof in admixture with a pharmaceutical carrier.

This invention also concerns compounds of formula

the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein L, Q, R³, R⁴, R⁵ and A are as defined under formula (I), and

R^(4′) is halo, C₁₋₆alkyl, cyano, aminocarbonyl, nitro, trihalomethyl, trihalomethyloxy or C₁₋₆alkyl substituted with cyano or aminocarbonyl; n′ is 0, 1, 2 or 3;

with the proviso that Q and L are other than anilino, 2,4,6-trinitro-anilino, 3-methoxy-anilino, 4-methoxy-anilino, 3,4-dimethoxy-anilino, 3-chloro-4-fluoro-anilino, 4-cyano-anilino, 2-(C₁₋₆alkyl)-anilino, 4-(C₁₋₆alkyl)-anilino, 3-chloro-anilino, 4-bromo-anilino, 4-nitro-anilino and 4-chloro-anilino.

As used in the foregoing definitions and hereinafter halo defines fluoro, chloro, bromo and iodo; C₁₋₄alkyl as a group or part of a group encompasses the straight and branched chained saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as, for example, methyl, ethyl, propyl, butyl and the like; C₁₋₆alkyl as a group or part of a group encompasses the straight and branched chained saturated hydrocarbon radicals as defined in C₁₋₄alkyl as well as the higher homologues thereof containing 5 or 6 carbon atoms such as, for example pentyl or hexyl: C₁₋₁₀alkyl as a group or part of a group group encompasses the straight and branched chained saturated hydrocarbon radicals as defined in C₁₋₆alkyl as well as the higher homologues thereof containing 7 to 10 carbon atoms such as, for example, heptyl, octyl, nonyl or decyl; C₁₋₁₂alkyl as a group or part of a group encompasses the straight and branched chained saturated hydrocarbon radicals as defined in C₁₋₁₀alkyl as well as the higher homologues thereof containing 11 or 12 carbon atoms such as, for example, undecyl, dodecyl and the like; C₁₋₄alkylidene as a group or part of a group defines bivalent straight and branched chained hydrocarbons having from 1 to 4 carbon atoms such as, for example, methylene, ethylidene, propylidene, butylidene and the like; C₁₋₄alkanediyl as a group or part of a group encompasses those radicals defined under C₁₋₄alkylidene as well as other bivalent straight and branched chained hydrocarbons having from 1 to 4 carbon atoms such as, for example, 1,2-ethanediyl, 1,3-propanediyl, 1,4-butanediyl and the like: C₃₋₇cycloalkyl as a group or part of a group is generic to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl: C₃₋₁₀alkenyl as a group or part of a group defines straight and branch chained hydrocarbon radicals containing one double bond and having from 3 to 10 carbon atoms such as, for example, 2-propenyl, 2-butenyl, 2-pentenyl, 3-pentenyl, 3-methyl-2-butenyl, 3-hexenyl, 3-heptenyl, 2-octenyl, 2-nonenyl, 2-decenyl and the like, whereby the carbon atom attached to the pyrimidine ring is preferably an aliphatic carbon atom; C₃₋₁₀alkynyl as a group or part of a group defines straight and branch chained hydrocarbon radicals containing one triple bond and having from 3 to 10 carbon atoms such as, for example, 2-propynyl, 2-butynyl, 2-pentynyl, 3-pentynyl, 3-methyl-2-butynyl, 3-hexynyl, 3-heptynyl, 2-octynyl, 2-nonynyl, 2-decynyl and the like, whereby the carbon atom attached to the pyrimidine ring is preferably an aliphatic carbon atom.

It is to be understood that the three substituents [L, Q and NR³(optionally substituted phenyl or pyridyl)] on the pyrimidine ring can be on any free position of the pyrimidine ring. Thus, given the following numbering of the pyrimidine ring

the three substituents may be connected to the pyrimidine ring in three different ways:

2-L, 4-Q, 6-NR³(optionally substituted phenyl or pyridyl); or

4-L, 2-Q, 6-NR³(optionally substituted phenyl or pyridyl); or

6-L, 4-Q, 2-NR³(optionally substituted phenyl or pyridyl).

The positions 4 and 6 are equivalent to one another. For instance, substitution pattern 6-L, 4-Q, 2-NR³(optionally substituted phenyl or pyridyl), which is a preferred substitution pattern, is equivalent to substitution pattern 4-L, 6-Q, 2-NR³(optionally substituted phenyl or pyridyl). Said subgroup of compounds is represented by formula

An interesting group of compounds are the compounds of formula

Of particular interest are those compounds of formula (I′-I) wherein L and Q are other than anilino, 2,4,6-trinitro-anilino, 4-(C₁₋₆alkyl)-anilino, 4-bromo-anilino, 4-nitro-anilino and 4-chloro-anilino; and of more particular interest are those compounds of formula (I′-I) wherein R^(4′) is cyano, aminocarbonyl or C₁₋₆alkyl substituted with cyano or aminocarbonyl.

The addition salts as mentioned herein are meant to comprise the therapeutically active addition salt forms which the compounds of the present invention are able to form with appropriate acids, such as, for example, inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic acid; sulfuric; nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic, maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-amino-salicylic, pamoic and the like acids.

The pharmaceutically acceptable addition salts as mentioned hereinabove are also meant to comprise the therapeutically active non-toxic base, in particular, a metal or amine addition salt forms which the compounds of the present invention are able to form. Said salts can conveniently be obtained by treating the compounds of the present invention containing acidic hydrogen atoms with appropriate organic and inorganic bases such as, for example, the ammonium salts, the alkali and earth alkaline metal salts, e.g. the lithium, sodium, potassium, magnesium, calcium salts and the like, salts with organic bases, e.g. the benzathine, N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like. Conversely said salt forms can be converted by treatment with an appropriate base or acid into the free acid or base form.

The term addition salts also comprises the hydrates and the solvent addition forms which the compounds of the present invention are able to form. Examples of such forms are e.g. hydrates, alcoholates and the like.

The term stereochemically isomeric forms of compounds of the present invention, as used hereinbefore, defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, at which the compounds of the present invention may possess. Unless otherwise mentioned or indicated, the chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound. All stereochemically isomeric forms of the compounds of the present invention both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.

Some of the compounds of the present invention may also exist in their tautomeric forms. Such forms although not explicitly indicated in the above formula are intended to be included within the scope of the present invention.

Whenever used hereinafter, the term “compounds of the present invention” is meant to include the compounds of formula (I), (I-I), (I′), (I′-I) or any subgroup thereof, also the N-oxides, the pharmaceutically acceptable addition salts and all stereoisomeric forms.

The group containing those compounds of the present invention wherein Q is NR¹R², each R⁴ independently is hydroxy, halo, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, amino-carbonyl, nitro, amino, trihalomethyl or trihalomethyloxy; L is C₁₋₁₀alkyl, C₃₋₁₀alkenyl, C₃₋₁₀alkynyl, C₃₋₇cycloalkyl, or C₁₋₁₀alkyl substituted with one or two substituents independently selected from C₃₋₇cycloalkyl, indolyl or indolyl substituted with one, two, three or four substituents each independently selected from halo, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl, trihalomethyloxy and C₁₋₆alkylcarbonyl, phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl, trihalomethyloxy and C₁₋₆alkyl-carbonyl; or L is —X¹—R⁶ wherein R⁶ is phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, C₁₋₆alkyl, C₁₋₆alkyloxy, C₁₋₆alkylcarbonyl, cyano, nitro and trifluoromethyl; is of interest.

Also of interest is the group containing those compounds of the present invention wherein Q is NR¹R²; each R⁴ independently is hydroxy, halo, C₁₋₆alkyl. C₁₋₆alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl or trihalomethyloxy; L is C₁₋₁₀alkyl substituted with one or two substituents independently selected from phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl, trihalomethyloxy and C₁₋₆alkylcarbonyl; or L is —X¹ —R⁶ wherein R⁶ is phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, C₁₋₆alkyl, C₁₋₆alkyloxy, C₁₋₆alkylcarbonyl, cyano, nitro and trifluoromethyl; with the proviso that compounds

(a) N2-hydroxy-N2-methyl-N4,N6-diphenyl-2,4,6-pyrimidinetriamine;

(b) N,N,N′,N′,N″,N″-hexakis(3-methylphenyl)-2,4,6-pyrimidinetriamine;

(c) N4-methyl-N2-(2-methylphenyl)-N4-phenyl-2,4,6-pyrimidinetriamine;

(d) N4-methyl-N2-(2-methylphenyl )-N4-phenyl-6-(phenylmethyl)-2,4-pyrimidine diamine;

(e) N4-(2-methylphenyl)-6-(phenylmethyl)-2,4-pyrimidinediamine;

(f) N,N′,N″-tris(4-methoxyphenyl)-2,4,6-pyrimidinetriamine;

(g) N,N′-bis(4-hexylphenyl )-6-(4-methoxyphenoxy)-2,4-pyrimidinediamine;

(h) N2N4-bis(4-hexylphenyl)-N6,N6-dimethyl-2,4,6-pyrimidinetriamine:

(i) N,N′,N″-tris(4-hexylphenyl)-2,4,6-pyrimidinetriamine;

(j) N2,N2-dimethyl-N4,N6-bis(4-methylphenyl)-2,4,6-pyrimidinetriamine;

(k) N,N′,N″-tris(4-methylphenyl)-2,4,6-pyrimidinetriamine;

(l) N,N′,N″-triphenyl-2,4,6-pyrimidinetriamine;

(m) N,N,N′,N′,N″,N″-hexakis(4-ethoxyphenyl)-2,4,6-pyrimidinetriamine;

(n) N4,N6-bis(2-chlorophenyl)-2,4,6-pyrimidinetriamine;

(o) N4,N6-bis(3-chlorophenyl)-2,4,6-pyrimidinetriamine;

(p) N4,N6-bis(2-ethoxyphenyl)-2,4,6-pyrimidinetriamine;

(q) N4,N6-bis(4-ethoxyphenyl)-2,4,6-pyrimidinetriamine;

(r) N4,N6-bis(2-methylphenyl)-2,4,6-pyrimidinetriamine;

(s) N4,N6-bis(4-bromophenyl)-2,4,6-pyrimidinetriamine;

(t) N4,N6-bis(4-methylphenyl)-2,4,6-pyrimidinetriamine;

(u) N2,N4-bis(4-methoxyphenyl)-2,4,6-pyrimidinetriamine;

(v) N2,N4-bis(4-methylphenyl)-2,4,6-pyrimidinetriamine;

(w) N,N′,N″-tris(2,4,6-trinitrophenyl)-2,4,6-pyrimidinetriamine;

(x) N4,N6-bis(4-chlorophenyl)-2,4,6-pyrimidinetriamine;

(y) N4,N6-bis(4-methoxyphenyl)-2,4,6-pyrimidinetriamine;

(z) N2,N4,N6-trimethyl-N2,N4,N6-triphenyl pyrimidine-2,4,6-triyltriamine;

(aa) N4,N4-dimethyl-N2,N6-di-p-tolyl-pyrimidine-2,4,6-triyltriamine; and

(bb) N2,N4-diphenyl-pyrimidine-2,4,6-triyltriamine are not included.

Suitably, Q may also be hydrogen in the above two groups of interest.

A special group of compounds are those compounds of formula (I) or (I′) wherein n is at least 1 and at least one R⁴ is cyano; preferably, n is 1 and R⁴ is cyano substituted in the para position relative to the NR³ moiety.

Another special group of compounds contains those compounds of formula (I) or (I′) which are other than

(c) N4-methyl-N2-(2-methylphenyl)-N4-phenyl-2,4,6-pyrimidinetriamine;

(d) N4-methyl-N2-(2-methylphenyl)-N4-phenyl-6-(phenylmethyl)-2,4-pyrimidine-diamine;

(e) N4-(2-methylphenyl)-6-(phenylmethyl)-2,4-pyrimidinediamine; the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof.

An interesting group of compounds are those compounds of the present invention wherein the NR³(substituted phenyl or pyridyl) moiety is in the 4- or 6-position of the pyrimidine ring.

Another interesting group are those compounds of the present invention wherein each R⁴ independently is hydroxy, halo, C₁₋₆alkyloxy, cyano, aminocarbonyl, nitro, amino, trihalomethyl or trihalomethyloxy; R⁶ is phenyl or phenyl substituted with one, two or three, four or five substituents each independently selected from halo, C₁₋₆alkyloxy, C₁₋₆alkylcarbonyl, cyano, nitro and trifluoromethyl; and aryl is phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, C₁₋₆alkyloxy, cyano, nitro and trifluoromethyl.

Suitably, Q is NR¹R² wherein R¹ is hydrogen, hydroxy, C₁₋₁₂alkyl, C₁₋₁₂alkyloxy, C₁₋₁₂alkylcarbonyl, C₁₋₁₂alkyloxycarbonyl, aryl, amino, mono- or di(C₁₋₁₂alkyl)amino, mono- or di(C₁₋₁₂alkyl)aminocarbonyl; and R² is hydroxy, C₁₋₁₂alkyl, C₁₋₁₂alkyloxy, C₁₋₁₂alkylcarbonyl, C₁₋₁₂alkyloxycarbonyl, aryl, amino, mono- or di(C₁₋₁₂alkyl)amino, mono- or di(C₁₋₁₂alkyl)aminocarbonyl; wherein each of the aforementioned C₁₋₁₂alkyl groups may optionally and each individually be substituted with one or two substituents each independently selected from hydroxy, C₁₋₆alkyloxy, hydroxyC₁₋₆alkyloxy, carboxyl, C₁₋₆alkyloxycarbonyl, cyano, amino, imino, aminocarbonyl, aminocarbonyl-amino, mono- or di(C₁₋₆alkyl)amino, aryl and Het; or R¹ and R² taken together may form pyrrolidinyl, piperidinyl, morpholinyl, azido or mono- or di(C₁₋₁₂alkyl)amino-C₁₋₄alkylidene.

Suitably, L is C₁₋₁₀alkyl substituted with one or two substituents independently selected from C₃₋₇cycloalkyl, indanyl, indolyl and phenyl, wherein said phenyl, indanyl and indolyl may be substituted with one, two, three, four or where possible five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, aminocarbonyl, C₁₋₆alkyloxycarbonyl, formyl, nitro, amino, trihalomethyl, trihalo-methyloxy and C₁₋₆alkylcarbonyl; or L is —X′—R⁶ or —X²-Alk-R′ and when X¹ is NR³, then R⁶ is phenyl substituted with one, two, three, four or five substituents each independently selected from C₁₋₆alkyloxycarbonyl, formyl, nitro and trihalomethyloxy.

Suitably, R⁴ or R^(4′) is nitro, trihalomethyloxy or C₁₋₆alkyl substituted with cyano or aminocarbonyl.

Suitably, R⁶ is phenyl or phenyl substituted with one, two, three, four or five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, C₁₋₆alkyloxycarbonyl, formyl, cyano, aminocarbonyl, nitro, amino, trihalomethyloxy and trihalomethyl.

Suitably, both Q and R⁵ are hydrogen.

Suitably, L is C₁₋₁₀alkyl substituted with one or two substituents independently selected from C₃₋₇cycloalkyl, indanyl, indolyl and phenyl, wherein said phenyl, indanyl and indolyl may be substituted with one, two, three, four or where possible five substituents each independently selected from halo, hydroxy, C₁₋₆alkyl, C₁₋₆alkyloxy, cyano, aminocarbonyl, C₁₋₆alkyloxycarbonyl, formyl, nitro, amino, trihalomethyl, trihalo-methyloxy and C₁₋₆alkylcarbonyl; or L is —X′—R⁶ or —X²-Alk-R⁷; and R⁵ is hydrogen.

Particular groups of compounds are those groups wherein one or more of the following conditions are met:

(i) n is 0, 1, 2 or 3;

(ii) Q is hydrogen;

(iii) Q is NR¹R² wherein R¹ and R² are each independently selected from hydrogen, hydroxy, C₁₋₁₂alkyl, C₁₋₁2alkyloxy, C₁₋₁₂alkylcarbonyl, C₁₋₁₂alkyloxycarbonyl, cyano wherein the aforementioned C₁₋₁₂alkyl groups may optionally and each individually be substituted with one or two substituents each independently selected from hydroxy, cyano, C₁₋₆alkyloxy, hydroxyC₁₋₆alkyloxy, aryl and Het; or R¹ and R² taken together may form mono- or di(C₁₋₁₂alkyl)aminoC₁₋₄alkylidene;

(iv) R³ is hydrogen or C₁₋₆alkyl;

(v) R⁴ is cyano, aminocarbonyl, amino, nitro, hydroxy, halo, C₁₋₆alkyl or cyanoC₁₋₆alkyl;

(vi) R⁴ is cyano, aminocarbonyl, halo, C₁₋₆alkyl or cyanoC₁₋₆alkyl;

(vii) R⁵ is hyrogen or methyl;

(viii) L is C₁₋₁₀alkyl substituted with phenyl substituted with one or two halogens; or L is —X¹—R⁶ wherein R⁶ is phenyl substituted with one, two or three substituents selected from C₁₋₆alkyl, trifluoromethyl, trifluoromethoxy, cyano, and halogen, and X¹ is —S—, —O— or —NR³—; or L is —X²-Alk-R⁷ wherein R⁷ is phenyl substituted with one, two or three substituents selected from C₁₋₆alkyl, cyano, and halogen and X² is NH.

Other particular compounds are those compounds of the present invention wherein L contains phenyl, 2,6-disubstituted-phenyl, 2,4,6-trisubstituted-phenyl or 2,3,4,5-tetra-substituted-phenyl;

especially, L contains phenyl, 2,4,6-trihalo-phenyl, 2,4,6-triC₁₋₄alkyl-phenyl, 2,3,4,5-tetrahalo-phenyl, 2,4-dihalo-6-C₁₋₄alkyl-phenyl, 2,6-dihalo4-C₁₋₄alkyl-phenyl, 2,6-dihalo-4-cyano-phenyl, 2,6-dihalo-4-trifluoromethoxy-phenyl, 2,6-dihalo-4-trifluoromethyl-phenyl, 2,6-diC₁₋₄alkyl-4-halo-phenyl, 2,6-diC₁₋₄alkyl-4-cyano-phenyl, 2,6-dihalo-phenyl or 2,6-diC₁₋₄alkyl-phenyl;

more in particular, L contains phenyl, 2,4,6-trichloro-phenyl, 2,4,6-trimethyl-phenyl, 2,4-dibromo-3,5-dichloro-phenyl, 2,4-dibromo-6-fluoro-phenyl, 2,4-dichloro-6-methyl-phenyl, 2,6-dibromo-4-isopropyl-phenyl, 2,6-dibromo-4-methyl-phenyl, 2,6-dibromo-4-prop-1-yl-phenyl, 2,6-dichloro-4-cyano-phenyl, 2,6-dichloro-4-trifluoromethoxy-phenyl, 2,6-dichloro4-trifluoromethyl-phenyl, 2,6-dichloro-phenyl, 2,6-dimethyl-4-(1,1-dimethylethyl)-phenyl, 2,6-dimethyl-phenyl, 2-bromo-4-fluoro-6-methyl-phenyl, 2-bromo-6-chloro-4-fluoro-phenyl, 4-bromo-2,6-dimethyl-phenyl, 4-chloro-2,6-dimethyl-phenyl, or 4-cyano-2,6-dimethyl-phenyl.

More particular compounds are the compounds of the present invention wherein L is 2,6-dichlorobenzyl, or L is —X¹—R⁶ wherein X¹ is —NR³—, —S—or —O— and R⁶ is 2,4,6-tri-chlorophenyl, 2,4,6-trimenthyl-phenyl, 2,4-dibromo-3,5-dichloro-phenyl, 2,4-dibromo-6-fluoro-phenyl, 2,4-dichloro-6-methyl-phenyl, 2,6-dibromo-4-isopropyl-phenyl, 2,6-dibromo-4-methyl-phenyl, 2,6-dibromo-4-prop-1-yl-phenyl, 2,6-dichloro-4-cyano-phenyl, 2,6-dichloro-4-trifluoromethoxy-phenyl, 2,6-dichloro-4-trifluoromethyl-phenyl, 2,6-dichloro-phenyl, 2,6-dimethyl-4-(1,1-dimethylethyl)-phenyl, 2,6-dimethyl-phenyl, 2-bromo-4-fluoro-6-methyl-phenyl, 2-bromo-6-chloro-4-fluoro-phenyl, 4-bromo-2,6-dimethyl-phenyl, 4-chloro-2,6-dimethyl-phenyl, 4-cyano-2,6-dimethyl-phenyl; or L is —X²-Alk-R⁷ wherein —X²-Alk- is —NH—CH₂— and R⁷ phenyl.

Still other particular compounds are those compounds of formula (I) where R³ is hydrogen, A is CH, n is 1, and R⁴ is halo, methyl or cyano and is positioned in the 4 position of the phenyl ring.

Preferred compounds are those compounds of the present invention wherein L is 2,6-dichlorobenzyl and the NR³(optionally substituted phenyl or pyridyl) moiety represents p-cyano-anilino and is in the 2 position of the pyrimidine ring.

Other preferred compounds are those compounds of the present invention wherein Q is hydrogen. L is —X¹—R⁶ wherein X¹ is —NH— and R⁶ is 2,4,6-trimethyl-phenyl or 4-cyano-2,6-dimethylphenyl, the NR³(optionally substituted phenyl or pyridyl) moiety represents p-cyano-anilino and is in the 2 position of the pyrimidine ring.

Still other preferred compounds are those compounds of the present invention wherein L is —X²-Alk-R⁷ wherein X² is —NH—, Alk is methylene and R⁷ is phenyl, 2,6-dichloro-phenyl, 2,4,6-trimethyl-phenyl or 4-cyano-2,6-dimethylphenyl.

More preferred are those compounds of formula (I′-I) wherein R^(4′) is halo, cyano, aminocarbonyl or cyanoC₁₋₆alkyl; n is zero, A is CH, R³ is hydrogen; R⁵ is hydrogen or methyl; Q is hydrogen or NHR¹; and L contains phenyl, 2,4,6-trichloro-phenyl, 2,4,6-trimethyl-phenyl, 2,4-dibromo-3,5-dichloro-phenyl, 2,4-dibromo-6-fluoro-phenyl, 2,4-dichloro-6-methyl-phenyl, 2,6-dibromo-4-isopropyl-phenyl, 2,6-dibromo-4-methyl-phenyl, 2,6-dibromo-4-prop-1-yl-phenyl, 2,6-dichloro4-cyano-phenyl, 2,6-dichloro-4-trifluoromethoxy-phenyl, 2,6-dichloro-4-trifluoromethyl-phenyl, 2,6-dichloro-phenyl, 2,6-dimethyl-4-(1,1-dimethylethyl)-phenyl, 2,6-dimethyl-phenyl, 2-bromo-4-fluoro-6-methyl-phenyl, 2-bromo-6-chloro-4-fluoro-phenyl, 4-bromo-2,6-dimethyl-phenyl, 4-chloro-2,6-dimethyl-phenyl, or 4-cyano-2,6-dimethyl-phenyl.

Most preferred are

4-[[4-amino-6-[(2,6-dichlorophenyl)methyl]-2-pyrimidinyl]amino]benzonitrile;

6-[(2,6-dichlorophenyl)methyl]-N2-(4-fluorophenyl)-2,4-pyrimidinediamine;

4-[[4-[(2,4-dichlorophenyl)methyl]-6-[(4-hydroxybutyl)amino]-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-[(3-hydroxypropyl)amino]-2-pyrimidinyl]amino]-benzonitrile;

N-[2-[(4-cyanophenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-4-pyrimidinyl]-acetamide;

N-[2-[(4-cyanophenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-4-pyrimidinyl]-butanamide;

4-[[2-amino-6-(2,6-dichlorophenoxy)-4-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-[(2-hydroxy-2-phenylethyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-[[3-(2-oxo-1-pyrrolidinyl)propyl]amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-[[2-(2-hydroxyethoxy)ethyl]amino]-2-pyrimidinyl]amino]benzontrile monohydrochloride;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-[(2,3-dihydroxypropyl)amino]-2-pyrimidinyl]-amino]benzonitrile;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-(hydroxyamino)-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[(2-cyanoethyl)amino]-6-[(2,6-dichlorophenyl)methyl]-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[(2,6-dichlorophenyl)methyl]-6-[[2-(1-pyrrolidinyl)ethyl]amino]-2-pyrimidinyl]-amino]benzonitrile;

4-[[4-amino-6-[(2,6-dichlorophenyl)methyl]-5-methyl-2-pyrimidinyl]amino]-benzonitrile;

N2-(4-bromophenyl)-6-[(2,6-dichlorophenyl)methyl]-5-methyl-2,4-pyrimidinediamine;

4-[[4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[2-[(2,4,6-trimethylphenyl)amino]-4-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-(2,4,6-trimethylphenoxy)-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dichlorophenyl)thio]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[[2,6-dibromo-4-(1-methylethyl)phenyl]amino]-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[[2,6-dichloro-4-(trifluoromethyl)phenyl]amino]-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[(2,4-dichloro-6-methylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[2-[(cyanophenyl)amino]-4-pyrimidinyl]amino]-3,5-dimethylbenzonitrile;

4-[[4-[(2,4-dibromo-6-fluorophenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-amino-6-[(2,6-dichlorophenyl)methyl]-5-methyl-2-pyrimidinyl]amino]-benzeneacetonitrile;

4-[[4-[methyl(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,4,6-trichlorophenyl)amino]-2-pyrimidinyl]amino]benzontrile;

4-[[4-[(2,4,6-trimethylphenyl)thio]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,4,6-trimethylphenyl)amino-2-pyrimidinyl]amino]benzonitrile;

4-[[4-amino-6-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[2-amino-6-[(2,4,6-trimethylphenyl)amino]-4-pyrimidinyl]amino]benzonitrile;

4-[[4-(2-bromo-4-chloro-6-methylphenoxy)-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(4-chloro-2,6-dimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

3,5-dichloro-4-[[2-[(4-cyanophenyl)amino]-4-pyrimidinyl]amino]benzonitrile;

4-[[4-[[2,6-dichloro-4-(trifluoromethoxy)phenyl]amino]-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[(2,4-dibromo-3,6-dichlorophenyl)amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dibromo-4-propylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzamide;

4-[[4-[(4-(1,1-dimethylethyl)-2,6-dimethylphenyl)amino]-2-pyrimidinyl]amino]-benzonitrile;

4-[[2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethylbenzonitrile;

4-[[4-[(4-chloro-2,6-dimethylphenyl)amino]-5-methyl-2-pyrimidinyl]amino]-benzonitrile;

4-[[2-[(4-cyanophenyl)amino]-5-methyl-4-pyrimidinyl]amino-3,5-dimethyl-benzonitrile;

4-[[4-[[4-(1,1-dimethylethyl)-2,6-dimethylphenyl]amino]-5-methyl-2-pyrimidinyl]-amino]benzonitrile;

4-[[4-[(4-bromo-2,6-dimethylphenyl)amino]-5-methyl-2-pyrimidinyl]amino]-benzonitrile;

4-[[5-methyl-4-[(2,4,6-trimethylphenyl)thio]-2-pyrimidinyl]amino]benzonitrile;

4-[[4-[(2,6-dibromo-4-propylphenyl)amino]-5-methyl-2-pyrimidinyl]amino]-benzonitrile;

4-[[4-[(2,4,6-trimethylphenyl)amino]-2pyrimidinyl]amino]benzamide, N3-oxide;

N2-(4-chlorophenyl)-N4-(2,4,6-trimethylphenyl)-2,4-pyrimidinediamine;

4-[[4-[[2,6-dibromo-4-(1-methylethyl)phenyl]amino]-5-methyl-2-pyrimidinyl]amino]-benzonitrile;

4-[[2-[(4-cyanophenyl)amino]-5-methyl4-pyrimidinyl]amino]-3,5-dimethyl benzonitrile;

4-[[4-[(phenylmethyl)amino]-2-pyrimidinyl]amino]benzonitrile; the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof.

The compounds of formula (I) can be prepared according to art-known procedures.

In particular, compounds of formula (I′) can generally be prepared by reacting an intermediate of formula (II-A) wherein W¹ is a suitable leaving group such as, for example, a halogen, with an amino derivative of formula (III) optionally in a solvent such as, for example, water, 2-propanol, diethylether, 1-methyl-2-pyrrolidinone and the like, and optionally in the presence of an acid such as, for example, 1 N hydrochloric acid in diethylether. It may be convenient to perform the reaction under a reaction-inert atmosphere such as, for example, oxygen free argon or nitrogen.

In this and the following preparations, the reaction products may be isolated from the reaction medium and, if necessary, further purified according to methodologies generally known in the art such as, for example, extraction, crystallization, distillation, trituration and chromatography.

Analogously to the reaction procedure described above, H-NR¹R² (VI) can also be reacted with an intermediate of formula (II-B).

Suitable solvents for the above reaction include, for instance, 2-propanol or 1,4-dioxane.

In case Q is NR¹R² and R² contains a hydroxy moiety, it may be convenient to perform the above reaction with a protected form of intermediate (VI) whereby the hydroxy moiety bears a suitable protecting group P being, for instance, a benzyl, and subsequently removing the protective group according to art-known methodologies, such as, for example, reacting with BBr₃ in dichloromethane under nitrogen atmosphere.

It is also possible to react H—X¹—R⁶ with an intermediate of formula (II-C) in a suitable solvent such as, for example, 1,4-dioxane, thus obtaining compounds of formula (I′) wherein L is —X¹—R⁶, said compounds being represented by formula (I′-c).

Depending on the nature of X¹ a suitable base or acid may be used to improve the reaction rate. For instance, in case X¹ is —O—, sodium hydride may be used as suitable base; or in case X¹ is NR³, HCl may be used as a suitable acid.

The compounds of formula (I′) may further be prepared by converting compounds of formula (I′) into each other according to art-known group transformation reactions.

For instance, compounds of formula (I′) whereby Q is NR¹R² and R¹ and R² are taken together to form mono- or di(C₁₋₁₂alkyl)aminoC₁₋₄alkylidene, said compounds being represented by formula (I′-a), may be prepared by reacting a compound of formula (I′) wherein R¹ and R² are hydrogen, with an intermediate of formula (IV) or a functional derivative thereof.

Also, compounds of formula (I′) wherein Q is NR¹R² and R¹ and R² are hydrogen may further be reacted with an acyl halide or an alkyl chloroformate in a reaction-inert solvent such as, for example dichloromethane, in the presence of a suitable base, such as, for example, pyridine, to form the corresponding amide, respectively, carbamate derivative.

Some of the compounds of formula (I′) and some of the intermediates in the present invention may contain an asymmetric carbon atom. Pure stereochemically isomeric forms of said compounds and said intermediates can be obtained by the application of art-known procedures. For example, diastereoisomers can be separated by physical methods such as selective crystallization or chromatographic techniques, e.g. counter current distribution, liquid chromatography and the like methods. Enantiomers can be obtained from racemic mixtures by first converting said racemic mixtures with suitable resolving agents such as, for example, chiral acids, to mixtures of diastereomeric salts or compounds; then physically separating said mixtures of diastereomeric salts or compounds by, for example, selective crystallization or chromatographic techniques, e.g. liquid chromatography and the like methods; and finally converting said separated diastereomeric salts or compounds into the corresponding enantiomers. Pure stereochemically isomeric forms may also be obtained from the pure stereochemically isomeric forms of the appropriate intermediates and starting materials, provided that the intervening reactions occur stereospecifically.

An alternative manner of separating the enantiomeric forms of the compounds of formula (I′) and intermediates involves liquid chromatography, in particular liquid chromatography using a chiral stationary phase.

The above specified reaction procedures for the preparation of compounds of formula (I′) or subgroups thereof, can also be applied for the preparation of compounds of formula (I).

Some of the intermediates and starting materials are known compounds and may be commercially available or may be prepared according to art-known procedures.

Intermediates of formula (II-A) wherein Q is NR¹R², said intermediates being represented by formula (II-A-I), can be prepared by reacting a pyrimidine derivative of formula (V) wherein W² is a suitable leaving group such as, for example, a halogen, with HNR¹R² (VI) in a reaction inert solvent such as, for example, 1,4-dioxane, 2-propanol or the like. Different regio-specific isomers may be formed and can be separated from one another using suitable separation techniques such as, for example, chromatography.

Intermediates of formula (II-B) can be prepared analogously to the preparation of compounds of formula (I′) starting from intermediates (II-A) and (III).

A particular subgroup of the intermediates of formula (II-B) is represented by formula

Particular intermediates of formula (II′-B) are those wherein W¹ is a halogen, more in particular, a chloro atom.

Intermediates of formula (V) whereby Q is NR¹R² and the L is L′-CH₂ and is attached in the 2 position of the pyrimidine ring and W² is chloro, said intermediates being represented by formula (V-a), can be prepared by reacting an imidamide of formula (VII) with a propanedioic acid ester of formula (VIII) in a solvent such as, for example, ethanol, and in the presence of, for instance, sodium, and subsequently reacting the thus formed intermediate of formula (IX) with a suitable reagent such as, for example, phosphoryl chloride.

Intermediates of formula (V) whereby Q is NR¹R² and L is L′-CH₂ and is attached in the 4 or 6 position of the pyrimidine ring and W² is chloro, said intermediates being represented by formula (V-b). can be prepared by reacting an intermediate of formula (X) with urea or a functional derivative thereof, in a solvent such as, for example, ethanol, and in the presence of, for instance, sodium, and subsequently reacting the thus formed intermediate of formula (XI) with a suitable reagent such as, for example, phosphoryl chloride.

Intermediates of formula (V) wherein Q is NR¹R² and L is L′-CH₂ and is attached anywhere on the pyrimidine ring, said intermediates being represented by formula (V-c), can be prepared by reacting an intermediate of formula (XII-1), for Q is NR¹R² and formula (XII-2) for Q is hydrogen, wherein W is a suitable leaving group such as, for example, a halogen, with an intermediate of formula (XIII) wherein W³ is a suitable leaving group such as, for example, a halogen, according to the procedure of a Grignard reaction.

Intermediates of formula (V) whereby Q is NR¹R² and L is —O—R⁶ or —NH—R and is attached in the 4 or 6 position of the pyrimidine ring, said intermediates being represented by formula (V-d), can be prepared by reacting an intermediate of formula (XIV) with an intermediate of formula (XII) wherein W² is a suitable leaving group such as, for example, a halogen, in a reaction-inert solvent such as, for example, tetrahydrofuran or 1,4-dioxane, and in the presence of a suitable base such as, for example, potassium hydroxide or diisopropyl ethaneamine, or sodium hydride.

The intermediates of formula (V-a) to (V-d) can analogously be prepared for the compounds of formula (I′) wherein Q is hydrogen. To this effect, there is one leaving group W² less on the pyrimidine ring of the respective starting material.

Compounds of formula (I′) and some of the intermediates may have one or more stereogenic centers in their structure, present in a R or a S configuration.

The compounds of formula (I′) as prepared in the hereinabove described processes may be synthesized as a mixture of stereoisomeric forms, in particular in the form of racemic mixtures of enantiomers which can be separated from one another following art-known resolution procedures. The racemic compounds of formula (I) may be converted into the corresponding diastereomeric salt forms by reaction with a suitable chiral acid. Said diastereomeric salt forms are subsequently separated, for example, by selective or fractional crystallization and the enantiomers are liberated therefrom by alkali. An alternative manner of separating the enantiomeric forms of the compounds of formula (I) involves liquid chromatography using a chiral stationary phase. Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically. Preferably if a specific stereoisomer is desired, said compound will be synthesized by stereospecific methods of preparation. These methods will advantageously employ enantiomerically pure starting materials.

The compounds of the present invention and the intermediates of formula (II′-B) show antiretroviral properties, in particular against Human Immunodeficiency Virus (HIV), which is the aetiological agent of Acquired Immune Deficiency Syndrome (AIDS) in humans. The HIV virus preferentially infects human T-4 cells and destroys them or changes their normal function, particularly the coordination of the immune system. As a result, an infected patient has an everdecreasing number of T-4 cells, which moreover behave abnormally. Hence, the immunological defense system is unable to combat infections and neoplasms and the HIV infected subject usually dies by opportunistic infections such as pneumonia, or by cancers. Other conditions associated with HIV infection include thrombocytopaenia. Kaposi's sarcoma and infection of the central nervous system characterized by progressive demyelination, resulting in dementia and symptoms such as, progressive dysarthria, ataxia and disorientation. HIV infection further has also been associated with peripheral neuropathy, progressive generalized lymphadenopathy (PGL) and AIDS-related complex (ARC).

The present compounds also show activity against HIV-1 strains that have acquired resistance to art-known non-nucleoside reverse transcriptase inhibitors. They also have little or no binding affinity to human α-1 acid glycoprotein.

Due to their antiretroviral properties, particularly their anti-HIV properties, especially their anti-HIV-1 -activity, the compounds of the present invention are useful in the treatment of individuals infected by HIV and for the prophylaxis of these individuals. In general, the compounds of the present invention may be useful in the treatment of warm-blooded animals infected with viruses whose existence is mediated by, or depends upon, the enzyme reverse transcriptase. Conditions which may be prevented or treated with the compounds of the present invention, especially conditions associated with HIV and other pathogenic retroviruses, include AIDS, AIDS-related complex (ARC), progressive generalized lymphadenopathy (PGL), as well as chronic CNS diseases caused by retroviruses, such as, for example HIV mediated dementia and multiple sclerosis.

The compounds of the present invention or any subgroup thereof may therefore be used as medicines against above-mentioned conditions. Said use as a medicine or method of treatment comprises the systemic administration to HIV-infected subjects of an amount effective to combat the conditions associated with HIV and other pathogenic retroviruses, especially HIV-1.

The compounds of the present invention or any subgroup thereof may be formulated into various pharmaceutical forms for administration purposes. As appropriate compositions there may be cited all compositions usually employed for systemically administering drugs. To prepare the pharmaceutical compositions of this invention, an effective amount of the particular compound, optionally in addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirable in unitary dosage form suitable, particularly, for administration orally, rectally, percutaneously, or by parenteral injection. For-example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employed such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules, and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit forms, in which case solid pharmaceutical carriers are obviously employed. For parenteral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations. In the compositions suitable for percutaneous administration, the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not introduce a significant deleterious effect on the skin.

It is especially advantageous to formulate the aforementioned pharmaceutical compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Examples of such dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions and the like, and segregated multiples thereof.

Those of skill in the treatment of HIV-infection could determine the effective daily amount from the test results presented here. In general it is contemplated that an effective daily amount would be from 0.01 mg/kg to 50 mg/kg body weight, more preferably from 0.1 mg/kg to 10 mg/kg body weight. It may be appropriate to administer the required dose as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 1 to 1000 mg, and in particular 5 to 200 mg of active ingredient per unit dosage form.

The exact dosage and frequency of administration depends on the particular compound of formula (I) used, the particular condition being treated, the seventy of the condition being treated, the age, weight and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention. The effective daily amount ranges mentioned hereinabove are therefore only guidelines and are not intended to limit the scope or use of the invention to any extent.

Also, the combination of an antiretroviral compound and a compound of the present invention can be used as a medicine. Thus, the present invention also relates to a product containing (a) a compound of the present invention, and (b) another antiretroviral compound, as a combined preparation for simultaneous, separate or sequential use in anti-HIV treatment. The different drugs may be combined in a single preparation together with pharmaceutically acceptable carriers. Said other antiretroviral compounds may be known antiretroviral compounds such as nucleoside reverse transcriptase inhibitors, e.g. zidovudine (3′-azido-3′-deoxythymidine, AZT), didanosine (dideoxy inosine; ddI), zalcitabine (dideoxycytidine, ddC) or lamivudine (3′-thia-2′-3′-dideoxycytidine, 3TC) and the like; non-nucleoside reverse transciptase inhibitors such as suramine, foscarnet-sodium (trisodium phosphono formate), nevirapine (11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b: 2′,3′-e] [1,4]diazepin-6-one), sustiva (efavirenz), tacrine (tetrahydroaminoacridine) and the like; compounds of the TIBO (tetrahydro-imidazo[4,5,1-jk] [1,4]-benzodiazepine-2(1H)-one and thione)-type e.g. (S)-8-chloro-4,5,6,7-tetrahydro-5-methyl-6-(3-methyl-2-butenyl)imidazo-[4,5,1-jk] [1,4 ]benzodiazepine-2(1H)-thione; compounds of the α-APA (α-anilino phenyl acetamide) type e.g. α-[(2-nitro-phenyl)amino]-2,6-dichloro-benzene-acetamide and the like; TAT-inhibitors, e.g. RO-5-3335 and the like; protease inhibitors e.g,. indinavir, ritanovir, saquinovir and the like; NMDA receptor inhibitors e.g. pentamidine: α-glycosidase inhibitor e.g. castanospermine and the like; Rnase H inhibitor e.g. dextran (dextran sulfate) and the like; or immunomodulating agents, e.g. levarnisole, thymopentin and the like.

The following examples are intended to illustrate the present invention.

Experimental Part

A. Intermediate Compounds

EXAMPLE A 1

a) A solution of 2,6-dichlorobenzylchloride (0.102 mol) in 1,1-diethylether (10 ml) was added dropwise to magnesium (0.102 mol) in 1,1-diethylether (60 ml). The reaction was initiated by adding 2 drops of 1,2-dibromoethane. After most of magnesium disappeared, 2,4,6-trichloropyrimidine (0.051 mol) in 1,1-diethylether (30 ml) was added. The mixture was stirred overnight at room temperature. The solvent was evaporated and the residue was purified by flash column chromatography over silica gel (eluent: CH₂Cl₂/hexane ½). The desired fractions were collected and the solvent was evaporated, yielding 3.3 g of (21%) 2,4-dichloro-6-[(2,6-dichloro-phenyl)methyl]pyrimidine (interm. 1; m.p.: 106-107° C.).

b) Intermediate (1) (0.0081 mol) in 2-propanol (100 ml) was heated until complete dissolution. The solution was then transferred into a pressure tube and NH₃ gas was bubbled into it for 20 minutes. Then the mixture was heated to 80° C. for 16 hours. The solvent was evaporated, yielding a residue of two compounds: 2-chloro-6-[(2,6-di-chloro-phenyl)methyl]-4-pyrimidinamine (interm. 2) and 4-chloro-6-[(2,6-dichloro-phenyl)methyl]-2-pyrimidinamine (interm. 3).

EXAMPLE A2

a) Urea (0.03 mol) was added to a mixture of (±)-ethyl 2,6-dichloro-phenyl-α-methyl-β-oxobutanoate (0.02 mol) in NaOC₂H₅ in ethanol, (1M; 0.040 mol; 40 ml). The reaction mixture was stirred and refluxed overnight. The solvent was evaporated, water was added and the mixture was neutralized with 0.3 N HOAc. The precipitate was filtered off and was further triturated with ether and then H₂O, then filtered off and dried, yielding 2.2 g (39%) of 6-[(2,6-dichloro-phenyl)methyl]-5-methyl-2,4(1H,3H)-pyrimidinedione (interm. 4).

b) A mixture of intermediate (4) (0.0095 mol) in phosphoryl chloride (50 ml) was stirred and refluxed overnight. Excess of phosphoryl chloride was then evaporated. Ice-water was added to the residue. A white precipitate was formed, filtered off and dried. The residue was purified by flash column chromatography over silica gel (eluent: CH₂Cl₂). The desired fractions were collected and the solvent was evaporated, yielding 2.06 g (67%) of 2,4-dichloro-6-[(2,6-dichloro-phenyl)methyl]-5-methyl-pyrimidine (interm. 5).

c) 4-chloro-6-[(2,6-dichloro-phenyl)methyl]-5-methyl-2-pyrimidinamine (interm. 6) and

2-chloro-6-[(2,6-dichloro-phenyl)methyl]-5-methyl-4-pyrimidinamine (interm. 7) were prepared from intermediate 5 following the procedures as described in example A1b.

EXAMPLE A3

a) To the stirred solution of 2,6-dichlorobenzeneethanimidamide HCl (1:1), (0.0042 mol) in ethanol (20 ml), a solution of sodium (0.013 mol) in ethanol (10 ml) was added dropwise first and then propanedioic acid, diethyl ester (0.0109 mol) was added. The reaction mixture was stirred and refluxed for 4 hours and then stirred at room temperature overnight After adding another equivalent of propanedioic acid, diethyl ester (stirring and refluxing it overnight), the solvent was evaporated and the residue was dissolved in water and acidified with 1 N HCl. The solid was filtered off, washed with water and dried, yielding 0.87 g (76.4%) of 2-[(2,6-dichloro-phenyl)methyl]-4,6-pyrimidinediol (interm. 8).

b) 6-chloro-2-[(2,6-dichloro-phenyl)methyl]4-pyrimidinamine (interm. 9) was prepared starting from intermediate 8 according to the procedures described in example A.1.b, A2.b & A2.c.

EXAMPLE A4

4-Amino-1-butanol (1.57 ml) was added to a solution of intermediate (1) (0.008 mol) in 1,4-dioxane (20 ml) under Argon. The reaction mixture was stirred for 2 hours at room temperature. The solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH₂Cl₂/CH₃OH: from 100/0 to 98/2). The pure fractions were collected and the solvent was evaporated, yielding 2.05 g of a mixture of 4-[[2-chloro-6-[(2,6-dichloro-phenyl)methyl]-4-pyrimidinyl]-amino]-1-butanol (interm. 10) and 4-[[4-chloro-6-[(2,6-dichloro-phenyl)methyl]-2-pyrimidinyl]amino]-1-butanol (interm. 11).

EXAMPLE A5

a) Potassium hydroxide/ethanol (10%; 0.035 mol) was added to a solution of 2,6-dichlorophenol (0.035 mol) in tetrahydrofuran (100 ml). The mixture was stirred and 2,4,6-trichloropyrimidine (0.044 mol) was added. The mixture was stirred overnight at 60° C. The reaction was quenched with NaOH 1N solution. The aqueous layers were extracted with EtOAc several times and then the organic layers were combined and washed with NaOH 3N and saturated NaCl, dried and concentrated. The residue was recrystallized from CH₂Cl₂/hexane. The precipitate was filtered off and dried, yielding 5.98 g 2,4-dichloro-6-(2,6-dichlorophenoxy)pyrimidine (55%) (interm. 12).

b) Reaction under Argon atmosphere, 2,4,6-trimethylaniline (0.0678 mol) was added to 2,4-dichloropyrimidine (0.0664 mol) in 1,4-dioxane (100 ml). N,N-di(1-methylethyl)-ethaneamine (0.0830mol) was added. The reaction mixture was stirred and refluxed for 4days and the solvent was evaporated. The residue was dissolved in CH₂Cl₂, washed with a saturated NaHCO₃ solution, then dried (Na₂SO₄), filtered and the solvent was evaporated to give 17.1 g solid residue. This solid was dissolved in CH₂Cl₂:hexane (1:1; 150 ml), and the resulting solution was concentrated to 100 ml, then filtered. The residue was purified by column chromatography on KP-Sil (eluent: CH₂Cl₂). The desired fractions were collected and the solvent was evaporated. The less polar fraction was stirred in CH₂Cl₂ for 3 hours and filtered, yielding 0.44 g 4-chloro-N-(2,4,6-tri-methylphenyl)-2-pyrimidinamine (intermediate 48). A second fraction was recrystallized from acetonitrile, filtered off and dried, yielding 2-chloro-N-(2,4,6-trimethyl-phenyl)-4-pyrimidinamine (intermediate 49).

EXAMPLE A6

Pyridine (1 ml) was added to a mixture of 4-[[4-amino-6-[(2,6-dichloro-phenyl)-methyl]-2-pyrimidinyl]amino]benzonitrile (0.00135 mol) in CH₂Cl₂ (19 ml). A solution of chloroethanoyl chloride (0.001375 mol) in CH₂Cl₂ (0.5 ml) was added dropwise on an ice bath. The mixture was stirred at room temperature for 2 hours. More chloroethanoyl chloride (0.00625 mol) in CH₂Cl₂ (0.5 ml) was added. The mixture stood in the refrigerator overnight. The solvent was evaporated. The residue was treated with a saturated Na₂CO₃ solution and the mixture was extracted with CH₂Cl₂. The separated organic layer was dried, filtered and concentrated. The residue was purified by flash column chromatography over silica gel (eluent: CH₂Cl₂/CH₃OH/NH₄OH 99/1/0.1). The desired fractions were collected and the solvent was evaporated, yielding 0.22 g (36.5%) of 2-chloro-N-[6-[(2,6-dichloro-phenyl)methyl]-2-[(4-cyano-phenyl)amino]-4-pyrimidinyl]acetamide (interm. 13).

EXAMPLE A7

A mixture of 4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile (0.005 mol) and nitryl tetrafluoroborate (0.0025 mol) in acetonitrile (5 ml) was stirred at room temperature for 4 h. The material was quenched with saturated bicarbonate (50 ml) on cracked ice. The mixture was allowed to reach room temperature, and the yellow solid was filtered off. The solid was adsorbed onto silica and purified by column chromatography (eluent: 30%, 50%, 60%, 70% CH₂Cl₂ in hexanes). The solvent of the desired fraction was evaporated and the residue was dried, yielding 0.89 g (64%) of 3-nitro-4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile.(interm. 51)

EXAMPLE A8

A mixture of 2,6-dichloro-N-(2,4,6-trimethylphenyl)-4-pyrimidinamine (0.00376 mol) in a 2.0 M solution of NH₃ in 2-propanol (25 ml) and a 0.5 M solution of NH₃ in dioxane (25 ml) was heated in a pressure sample at 110-115° C. for 24 hours. The solvent was evaporated, and the residue was chromatographed on Biotage (eluent: 1:1 CH₂Cl₂:hexane). The desired fractions were collected and the solvent was evaporated, yielding a mixture of 0.523 g of 2-chloro-N4-(2,4,6-trimethylphenyl)-4,6-pyrimidine-diamine (interm. 53) and 0.101 g of 6-chloro-N4-(2,4,6-trimethylphenyl)-2,4-pyrimidinediamine. (interm. 50)

Tables 1 and 2 list intermediates which were prepared analogous to one of the above examples. TABLE 1a

Int. Ex. physical data No. No. R^(a) R^(b) R^(c) X R⁵ R melting point 6 A2c Cl H Cl CH₂ CH₃ —NH₂ — 15 A1b Cl H Cl CH₂ H —NH—CH₃ — 16 A1b Cl H Cl O H —NH—CH₃ 152-155° C. 17 A1b Cl H Cl O H —NH₂ — 19 A4 Cl H Cl CH₂ H —NH—(CH₂)_(3—OH) — 20 A4 Cl H Cl CH₂ H —NR—(CH₂)_(2—OH) 111-113° C. 21 A4 CI H Cl CH₂ H —NH—CH₂—CH(OH)—C₆H₅ 133-134° C. 22 A4 Cl H Cl CH₂ H

— 23 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—O—(CH₂)₂OH  99-107° C. 24 A4 Cl H Cl CH₂ H —NR—(CH₂)₂—(4-OCH₃—C₆H₄₎ 138-140° C. 25 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(3-OCH₃—C₆H₄₎ 132-135° C. 26 A4 Cl H Cl CH₂ H —NH—CH₂—CH(OH)—CH₂OH 116-118° C. 27 A4 Cl H Cl CH₂ H —NH—CH₂—C₆H₅ 137-139° C. 28 A4 Cl H CI CH₂ H —NH—(CH₂)₂—(2-thienyl) 113-114° C. 29 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(2-pyridyl) 113.5-114° C.   31 A4 Cl H Cl CH₂ H —NH—(CH₂)₂CN 151-153° C. 48 A5b CH₃ CH₃ CH₃ NH H —H 142-143° C. 50 A8 CH₃ CH₃ CH₃ NH H —NH₂

TABLE 1b

Int. Ex. physical data No. No. R^(a) R^(b) R^(c) X R⁵ R melting point 14 A2b H CN H NH H H 211-212° C. 18 A5b CH₃ CH₃ CH₃ NH CH₃ H 30 A2b H CN H NH CH₃ H 51 A7 NO₂ CN H NH H H 142-144° C.

TABLE 2

Int. Ex. NO. No. R^(a) R^(b) R^(c) X R⁵ R physical data 7 A2c Cl H Cl CH₂ CH₃ —NH₂ 32 A1b Cl H Cl CH₂ H —NH—CH₃ — 33 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(1-pyrrolidinyl) 134-135° C. 34 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(2-pyridyl) 130-133° C. 35 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(2-thienyl) 98-99° C. 36 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(3-OCH₃—C₆H₄) 104-109° C. 37 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—(4-OCH₃—C₆H₄) 149-150° C. 38 A4 Cl H Cl CH₂ H —NH—(CH₂)₂CN 137-139° C. 39 A4 Cl H Cl CH₂ H —NH—(CH₂)₂—O—(CH₂)₂OH — 40 A4 Cl H Cl CH₂ H —NH—(CH₂)₂OH 170-173° C. 41 A4 Cl H Cl CH₂ H —NH—(CH₂)₃—O—CH(CH₃)₂ — 42 A4 Cl H Cl CH₂ H —NH—(CH₂)₃—OH — 43 A4 Cl H Cl CH₂ H —NH—CH2—C₆H₅ 171-172° C. 45 A4 Cl H Cl CH₂ H —NH—CH2—CH(OH)—CH₂OH >60° C. 46 A4 Cl H Cl CH₂ H —NH—O—CH2—C₆H₅ 137-141° C. 47 A4 Cl H Cl CH₂ H

55-60° C. 49 A5b CH₃ CH₃ CH₃ NH H H 182-183° C. 52 A4 Cl H Cl CH₂ H —NH—CH₂—CH(OH)—C₆H₅ 75-83° C. 53 A1b CH₃ CH₃ CH₃ NH H —NH₂ 54 A5b CH₃ CH₃ CH₃ NH CH₃ H 55 A5a Cl Cl Cl —O— H H 159-161° C.

B. Compounds of Formula (I′)

EXAMPLE B1

A mixture of intermediate (42) and intermediate (19) (0.004 mol) and 4-amino-benzonitrile (0.0084 mol) were combined in a sealed tube and heated for 16 hours at 160° C. under Argon. The reaction mixture was allowed to cool to room temperature and dissolved in CH₂Cl₂/CH₃OH 90/10 (20 ml) and 5 g of silica gel was added. After evaporating the solvent, the residue was purified by flash column chromatography over silica gel (eluent gradient: CH₂C₂/CH₃OH: from 100/0 to 97/3). The desired fraction was collected and the solvent was evaporated, yielding 0.31 g (18.1%) of 4-[[4-[(2,6-di-chloro-phenyl)methyl]-6- [(3-hydroxypropyl )amino]-2-pyrimidinyl]amino]benzonitrile (compound 3).

EXAMPLE B2

Intermediates (47) and (22) (0.00399 mol) and 4-aminobenzonitrile (0.0012 mol) in 1-methyl-2-pyrrolidinone (3 ml) was stirred for 16 hours at 130° C. under Argon. Then, the reaction mixture was cooled to room temperature and quenched with H₂O (200 ml). A precipitate formed, which was stirred for 16 hours, and separated by filtration over Celite. The residue was dissolved in CH₃OH/CH₂Cl₂ (10%, 200 ml), dried over K₂CO₃, filtered, and evaporated. This resulting material was further purified by flash column chromatography over silica gel (gradient eluent: CH₂Cl₂/CH₃OH from 100/0 to 95/5). The desired fraction was collected and the solvent was evaporated, yielding 0.43 g (21.7%) of 4-[[6-[(2,6-dichloro-phenyl)methyl]-2-[[3-(2-oxo-1-pyrrolidinyl)propyl]-amino]-4-pyrimidinyl]amino]benzonitrile (comp. 39: 104-114° C.).

EXAMPLE B3

HCl/diethyl ether (1 N; 2.77 ml) was stirred into a solution of intermediate (33) (0.00277 mol) in 1-methyl-2-pyrrolidinone (4 ml) under N₂ atmosphere. The reaction mixture was heated for 5 minutes. Next, 4-aminobenzonitrile (0.0061 mol) was added and the reaction was heated at 100° C. for 16 hours. Then, the reaction mixture was cooled to room temperature and diluted with ethylacetate (10 ml). The organic layer was washed with NaOH (1 N; 2×100 ml), H₂O (2×100 ml), brine (50 ml), respectively, dried, filtered and the filtrate was evaporated. The crude material was purified by flash chromatography (eluent: 2.5-7.5% of CH₃OH containing 10% NH₄OH in CH₂C₂). The desired fractions were collected and the solvent was evaporated. The residue was dried, yielding 0.160 g (12.0%) of 4-[[4-[(2,6-dichloro-phenyl)methyl]-6-[[2-(1-pyrrolidinyl)ethyl]amino]-2-pyrimidinyl]amino]benzonitrile (comp. 13: mp. 80-85° C.).

EXAMPLE B4

A slurry of intermediate (14) (0.005 mol) in CH₂Cl₂ (150 ml) was stirred rapidly and cooled to 0° C. under nitrogen. BBr₃ (0.015 mol) was introduced by syringe. The reaction mixture was stirred rapidly for two hours. The reaction mixture was recooled to 00° C. and quenched with NaOH (aq. 1 N, 25 ml). The biphasic partial quench mixture gives a precipitate which was filtered off and dried, yielding 2.5 g (91%) of 4-[[4-[(2,6-dichloro-phenyl)methyl]-6-(hydroxyamino)-2-pyrimidinyl]amino]-benzonitrile dihydrobromide, pentahydrate (comp. 15; mp. 240-244° C.).

EXAMPLE B5

1,1-Dimethoxy-N,N-dimethylmethanamine (0.152 mol) was added to 4-[[4-amino-6-[(2,6-dichlorophenyl)methyl]-2-pyrimidinyl]amino]benzonitrile (0.0008 mol). The mixture was stirred at room temperature for 2 days and then concentrated. The crude product was purified by flash chromatography over silica gel (eluent: CH₂Cl₂/CH₃OH 99/1). The desired fraction was collected and the solvent was evaporated. The resulting residue was triturated with hexane, yielding 0.15 g (42%) of N′-[2-[(4-cyano-phenyl)amino]-6-[(2,6-dichlorophenyl)methyl]-4-pyrimidinyl]-N,N-dimethyl-methanimidamide (comp. 26: mp. 175-180° C.).

EXAMPLE B6

Piperidine (0.12 ml) was added to a mixture of intermediate (13) (0.00047 mol) in terahydrofuran (20 ml). The mixture was stirred at room temperature for 4 hours. More piperidine (0.14 ml) was added. The mixture was stirred for another 2 hours. The solvent was evaporated. The residue was purified by flash column chromatography over silica gel (CH₂Cl₂/CH₃OH/NH₄OH 99/1/0.1). The desired fractions were collected and the solvent was evaporated, yielding 0.05 g (21.5%) of N-[6-[(2,6-di-chloro-phenyl)methyl]-2-[(4-cyano-phenyl)amino]-4-pyrimidinyl]-1-piperidine-acetamide (comp. 25: mp. 175-180° C.).

EXAMPLE B7

Pyridine (0.014 mol) was added to a mixture of 4-[[4-amino-6-[(2,6-dichlorophenyl)-methyl]-2-pyrimidinyl]amino]benzonitrile (0.0013 mol) in CH₂Cl₂. A solution of octanoyl chloride (1.5 equiv) in CH₂Cl₂ (0.5 ml) was added dropwise. The mixture was stirred at room temperature for 2 hours. More octanoyl chloride (3.5 equiv) in CH₂Cl₂ was added dropwise. The mixture was stirred. The solvent was then evaporated. The residue was treated with a saturated aqueous NaHCO₃ solution and the mixture was extracted with CH₂Cl₂. The separated organic layer was dried, filtered and the solvent was evaporated to give the crude product. The residue was recrystallized from CHCl₃ and hexane, yielding 0.443 g (68.6%) of N-[6-[(2,6-dichloro-phenyl)methyl]-2-[(4-cyano-phenyl)amino]-4-pyrimidinyl]octanamide (comp. 17: mp. 135-137° C.).

EXAMPLE B8

a) A mixture of intermediate 49 (0.082 mol) and 5.4 N HCl in 2-propanol (0.086 mol) in water (300 ml) was stirred and warmed to 40-45° C. over 30 minutes. 4-Amino-benzonitrile (0.242 mol) was added at 40-45° C. The reaction mixture was stirred and refluxed for 4.5 hours, then cooled to room temperature. The mixture was alkalized by portionwise addition of NaHCO₃. This mixture was extracted with ethylacetate. The organic layer was separated, washed with brine, dried, filtered and the solvent was evaporated. This fraction was stirred in ethanol p.a. (100 ml), filtered off, washed with ethanol (50 ml), then dried, yielding 23.1 g (86%) 4-[[4-[(2,4,6-trimethylphenyl)-amino]-2-pyrimidinyl]amino]benzonitrile (compound 52).

b) A mixture of 4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile (0.021 mol) and HCl in 2-propanol (0.0095 mol) in water (30 ml) was stirred for one hour at 45° C. 4-amino-3,5-dimethyl-benzonitrile (0.025 mol) was added and the reaction mixture was stirred and refluxed overnight. The mixture was cooled to room temperature, then neutralized with NaHCO₃. This mixture was extracted with ethylacetate. The separated organic layer was washed with brine, dried, filtered and the solvent evaporated. The residue was crystallized from CH₃CN, filtered off and dried. The residue was stirred in boiling CH₂Cl₂ (20 ml), then filtered off and dried. The residue was crystallized from methyl isobutyl keton, filtered off and dried, yielding 0.3 g of 4-[[2-[(cyanophenyl)amino]-4-pyrimidinyl]amino]-3,5-dimethylbenzonitrile (compound 69).

EXAMPLE B9

a) 4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile (0.003 mol), 2,6-dibromo-4-methyl-benzenamine (0.006 mol) and 1 M HCl in diethyl ether (4.5 ml) in 1,4-dioxane (10 ml) were combined in a tube and heated under Ar until all diethyl ether had evaporated. The tube was sealed and heated at 170° C. for 2.5 days. Silica gel was added, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH₂Cl₂:CH₃OH:NH₄OH 100:0:0 to 99:0.9:0.1). The desired fractions were collected and the solvent was evaporated. The residue was recrystallized from acetonitrile, filtered off and dried, yielding 0.22 g (15.9%) of 4-[[4-[(2,6-dibromo-4-methylphenyl )amino]-2-pyrimidinyl]amino]benzonitrile (compound 61).

b) 4-[[4-[(4-chloro-5-methyl-2-pyrimidinyl]amino]benzonitrile (0.01541 mol), 4-amino-3,5-dimethyl-benzonitrile (0.00219 mol), 1-methyl-2-pyrrolidinone (4 ml), 1,4-dioxane (15 ml) and diisopropylethylamine (0.0154 mol) were combined in a flask under a stream of argon and heated at 160-230° C. for 16 hours. CH₂Cl₂ and 1 N NaOH were added, and the mixture was stirred 1 hour and filtered to give a brown solid (*). The CH₂Cl₂ filtrate was separated and was evaporated and purified by flash column chromatography (eluent: 2% CH₃OH/CH₂Cl₂). The desired fractions were combined, evaporated and the residue was stirred in CH₂Cl₂. The solid precipitate was filtered off, combined with the brown solid (*) and recrystallized from CH₃CN. The precipitate was filtered off and dried, yielding 1.57 g (29%) of 4-[[2-[(4-cyanophenyl)amino]-5-methyl-4-pyrimidinyl]amino]-3,5-dimethylbenzonitrile ( compound 89).

c) 2-[(4-cyanophenyl)amino]-4-pyrimidinyl trifluoromethanesulfonate (0.0022 mol) and 2,6-dichloro-4-(trifluoromethyl)-benzenamine (0.0044 mol) were combined in 1,4-dioxane (2.5 ml) and heated in a sealed tube under Ar at 170° C. for 40 hours. The reaction mixture was allowed to cool to room temperature. Silica gel was added, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH₂Cl₂:CH₃OH:NH₄OH 100:0:0 to 97:2.7:0.3). The desired fractions were collected and the solvent was evaporated. The residue was recrystallized from CH₃CN, filtered off and dried, yielding 0.086 g (9.2%) of 4-[[4-[[2,6-dichloro-4-(trifluoromethyl)-phenyl]amino]-2-pyrimidinyl]amino]benzonitrile (compound 66).

EXAMPLE B10

To a suspension of NaH (0.006 mol) in 1,4-dioxane (30 ml), 2,4,6-trimethyl-phenol (0.006 mol) was added. The mixture was stirred for 15 minutes at room temperature, and a clear solution formed. 4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile (0.004 mol) was added, and the reaction mixture was heated to reflux under Argon for 15 hours. The reaction mixture was allowed to cool to room temperature, 0.5 ml of water was added, followed by 4 g of silica gel, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH₂Cl₂:CH₃OH 100:0:0 to 97:3). The pure fractions were collected and the solvent was evaporated, yielding 1.18 g (89.4%) of 4-[[4-(2,4,6-trimethylphenoxy)-2-pyrimidinyl]amino]benzonitrile (compound 58).

EXAMPLE B11

Compound (52) (0.0015 mol) was stirred in boiling ethanol (8 ml). 6 M HCl in 2-propanol (0.0015 mol) was added and the salt was allowed to crystallize out overnight at room temperature. The precipitate was filtered off, washed with 2-propanol and dried, yielding 0.47 g (86%) of 4-[[4-[(2,4,6-trimethyl-phenyl)amino]-2-pyrimidinyl]amino]benzonitrile hydrochloride (1:1) (compound 53).

EXAMPLE B12

A mixture of compound (52) (0.00303 mol) and NaBO₃.4H₂O (0.00911 mol) in CH₃OH (30 ml) and H₂O (10 ml) was stirred and refluxed for 4 days. The reaction mixture was cooled. The precipitate was filtered off and the precipitate (*) was purified by flash column chromatography over silica gel (eluent: CH₂Cl₂/CH₃OH gradient from 100/0 to 95/5). The desired fractions were collected and the solvent was evaporated, yielding 0.586 g (56%) of 4-[[4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzamide (compound 100). The filtrate (*) was purified by reversed-phase HPLC (eluent gradient: ((0.5% ammoniumacetate in H₂O)/CH₃CN 90/10)/CH₃OH/CH₃CN (0 minutes) 75/25/0, (44 minutes) 0/50/50, (57 minutes) 0/0/100, (61.1-70 minutes) 75/25/0). Three desired fraction groups were collected and their solvent was evaporated, yielding 0.18 g of 4-[[4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzamide. N3-oxide (compound 106) and 0.030 g of 4-[[4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzamide, N1-oxide compound 107).

Tables 3, 4, 5 and 6 list the compounds of formula (I) that were prepared according to one of the above examples. TABLE 3

physical data Co. (melting point No. No. NR¹R² in ° C.) 1 B2 —NH—(CH₂)₄—OH 161-163° C. 2 B2 —NH—(CH₂)₂—OH 207-210° C. 3 B2 —NH—(CH₂)₃—OH 152-154° C. 4 B2 —NH—CH₂—CHOH—C₆H₅ 158-165° C. 5 B2

48-56° C. 6 B2 —NH—(CH₂)₂—O—(CH₂)₂—OH 162-175° C.; HCl (1:1) 7 B2 —NH—(CH₂)₃—O—CH(CH₃)₂ 181-182° C.; HCl (1:1) 8 B2 —NH—(CH₂)₂—(3-OCH₃-C₆H₄) 72-80° C. 9 B2 —NH—CH_(2—CHOH—CH) ₂OH 189-192° C. 10 B2 —NH—(CH₂)₂—(4-OCH₃—C₆H₄) 72-80° C. 11 B2 —NH—O—CH₂—C₆H₅ — 12 B2 —NH—CH₂—C₆H₅ — 13 B3 —NH—(CH₂)₂-(1-pyrrolidinyl) 80-85° C. 14 B2 —NH—(CH₂)₂-(2-thienyl) — 15 B4 —NH—OH 240-244° C. 16 B2 —NH—(CH₂)₂—(2-pyridyl) 75-80° C. 17 B7 —NH—CO—C₇H₁₅ 135-137° C. 18 B7 —NH—CO—C₁₁H₂₃ 130-135° C. 19 B2 —NH—(CH₂)_(2—CN)  12 255° C.; HCl (1:1) 20 B7 —NH—CO13 O—C₂H₅ >200° C.  21 B7 —NH—CO—CH₃ 128-130° C. 22 B7 —NH—CO—C₃H₇ >200° C.  23 B —NH₂ 94-97° C. 24 BI —NH—CH₃ 170-180° C. 25 B6 —NH—CO—CH₂—(1-pipendinyl) 175-180° C. 26 B5 —NH═CH—N(CH₃)₂ 175-180° C.

TABLE 4

Co. Ex. Physical data No. No. R′ R″ R⁵ (melting point) 27 B1 4-Br—C₆H₄ H H — 28 B1 H 4-Br—C₆H₄ H — 29 B1 4-Cl—C₆H₄ H H — 30 B1 H 4-Cl—C₆H₄ H — 31 B1 H (3-Br—6-pyridyl) H — 32 B1 (3-Br—6-pyridyl) H H — 33 B1 4-F—C₆H₄ H H 77-80° C. 34 B1 H 4-F—C₆H₄ H >200° C. 35 B1 4-CH₃—C₆H₄ H H 76-79° C. 36 B1 H 4-CH₃—C₆H₄ H 183-186° C. 37 B1 C₆ ₅ H H 85-90° C. 38 B1 H C₆H₅ H 182-187° C. 39 B2

4-CN-C₆H₄ H 104-114° C. 40 B2 (CH₂₎ ₂—OH 4-CN-C₆H₄ H  247-250 ° C.; HCl (1:1) 41 B1 CH₃ 4-CN-C₆H₄ H >200 ° C. 42 B1 (CH₂)₃—OH 4-CN-C₆H₄ H  91-105° C. 43 B2 (CH₂)₄—OH 4-CN-C₆H₄ H 161-163° C. 45 B1 H 4-CN-C₆H₄ H >200 ° C. 46 B1 H 4-CN-C₆H₄ CH₃ >200 ° C. 47 B1 4-CN-C₆H₄ H CH₃ >200° C. 48 B1 H 4-Br-C₆H₄ CH₃ >200° C. 49 B1 4-Br-C₆H₄ H CH₃ 168-170° C.

TABLE 5

Co. Ex. physical No. No. R′ R″ R′″ R⁵ data 50 B1 NH₂ 4-CN—C₆H₄ O—(2,6-diCl-C₆H₃) H >200° C. 51 B1 CH₂—(2,6-diCl-C₆H₃) H —NH—(4-CN—C₆H₄) H >200 90 B9a NH—(2-NO₂-4—CN—C₆H₃) 2,4,6-triCH₃—C₆H₂ H H 165-168° C. 91 NH—(3-OH-4-CN—C₆H₃) 2,4,6-triCH₃—C₆H₂ H H 92 B12 NH—(2,6-diCl—C₆H₃) 2,6-diCl-C₆H₃ H H 164-166° C. 93 B9a NH—(2,4,6-triCH₃—C₆H₂) 4-CN—C₆H₄ H H 267-268° C. 94 B1 NH—(4-CN—C₆H₄) 2,4,6-triCH₃—C₆H₂ NH₂ H 263-264° C. 95 B1 NH₂ 2,4,6-triCH₃—C₆H₂ —NH—(4-CN—C₆H₄) H 233-234° C. 96 B8a NH—(4-Cl—C₆H₄) 2,4,6-triCH₃—C₆H₂ H H 97 B8a NH—(2,4-diF-C₆H₃) 2,4,6-triCH₃—C₆H₂ H H 98 B8a

2,4,6-triCH₃—C₆H₂ H H 99 B9a NH—(2,4,6-triCH₃—C₆H₂) 4-CN—C₆H₄ H CH₃ 200-201° C. 100 B11

2,4,6-triCH₃—C₆H₂ H H 101 B8a

2,4,6-triCH₃—C₆H₂ H H 102 B8a

2,4,6-triCH₃—C₆H₂ H H 103 B1

H —CH₂—(2,6-diCl—C₆H₃) CH₃ >200° C. 104 NH—(4-CN—C₆H₄) C₆H₅—CH₂— H H 105 NH—(2,4,6-triCH₃—C₆H₂) 2,4,6-triCH₃—C₆H₂ H H

TABLE 6

Co. Ex. physical data No. No. X R⁵ R^(6a) R^(6b) R^(6c) R^(6d) (salt form; melting point) 52 B8a NH H CH₃ H CH₃ CH₃ 217-218° C. 53 B11 NH H CH₃ H CH₃ CH₃ HCl (1:1) 54 B11 NH H CH₃ H CH₃ CH₃ HBr (1:1) 55 B11 NH H CH₃ H CH₃ CH₃ L-tartrare 56 B9a NH H CH₃ H Br CH₃ HCl (1:1); 214-217° C. 57 B9a NH H CH₃ H H CH₃ HCl (1:1); >270° C. 58 B10 O H CH₃ H CH₃ CH₃ 220-222° C. 59 B10 S H Cl H H Cl 225-226° C. 60 B3 O H Cl H Cl Cl 279-280° C. 61 B9a NH H Br H CH₃ Br 230-233° C. 62 B9a NH H Br H CH(CH₃)₂ Br 198-200° C. 63 B3 NH CH₃ CH₃ H CH₃ CH₃ 236-237° C. 64 B10 O H Cl H Cl CH₃ 266-267° C. 65 B9a NH H Cl H H Cl 253-255° C. 66 B9c NH H Cl H CF₃ Cl 239-240° C. 67 B9c NH H Br H F Cl 244-245° C. 68 B9a NH H Cl H Cl CH₃ 217° C. 69 B8b or NH H CH₃ H CN CH₃ 225-230° C. B9a 70 B9c NH H Br H Br F 210-214° C. 71 B9c N(CH₃) H CH₃ H CH₃ CH₃ 218-219° C. 72 B9c NH H Cl H Cl Cl trifluoroacetate (1:1); 225-230° C. 73 B10 S H CH₃ H CH₃ CH₃ 204.5-208° C. 74 B10 O H Br H Cl CH₃ 246-249° C. 75 B9c NH H CH₃ H Cl CH₃ 206-207° C. 76 B9a NH H Cl H CN Cl >180° C. 77 B9c NH H Cl H OCF₃ Cl 185-190° C. 78 B9c NH H Br Cl Br Cl >265° C. 79 B9c NH H Br H C3H7 Br 215-218° C. 80 B9a NH H CH₃ H C(CH₃)₃ CH₃ 203-205° C. 81 B10 O H CH₃ H CN CH₃ 279-280° C. 82 B9c NH CH₃ CH₃ H Cl CH₃ 235-237° C. 83 B9b NH CH₃ CH₃ H CN CH₃ H₂O (1:1) trifluoroacetace (1:1); 274-275° C. 84 B9c NH CH₃ CH₃ H C(CH₃)₃ CH₃ 231-232° C. 85 B9c NH CH₃ CH₃ H Br CH₃ 218-219° C. 86 B9c S CH₃ CH₃ H CH₃ CH₃ 229-230° C. 87 B9a NH CH₃ Br H C3H7 Br 197-198° C. 88 B9a NH CH₃ Br H CH(CH₃) Br 157-158° C. 89 B9b NH CH₃ CH₃ H CN CH₃ >300° C.

C. Pharmacological Example

Example C.1

A rapid, sensitive and automated assay procedure was used for the in vitro evaluation of anti-HIV agents. An HIV-1 transformed T4-cell line, MT-4, which was previously shown (Koyanagi et al., Int. J. Cancer, 36, 445-451, 1985) to be highly susceptible to and permissive for HIV infection, served as the target cell line. Inhibition of the HIV-induced cytopathic effect was used as the end point. The viability of both HIV- and mock-infected cells was assessed spectrophotometrically via the in situ reduction of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). The 50% cytotoxic concentration (CC₅₀ in μM) was defined as the concentration of compound that reduced the absorbance of the mock-infected control sample by 50%. The percent protection achieved by the compound in HIV-infected cells was calculated by the following formula: ${\frac{\left( {OD}_{T} \right)_{HIV} - \left( {OD}_{C} \right)_{HIV}}{\left( {OD}_{C} \right)_{MOCK} - \left( {OD}_{C} \right)_{HIV}}\quad{expressed}\quad{in}\quad\%},$

whereby (OD_(T))_(HIV) is the optical density measured with a given concentration of the test compound in HIV-infected cells: (OD_(C))_(HIV) is the optical density measured for the control untreated HIV-infected cells: (OD_(C))_(MOCK) is the optical density measured for the control untreated mock-infected cells: all optical density values were determined at 540 nm. The dose achieving 50% protection according to the above formula was defined as the 50% inhibitory concentration (IC₅₀ in μM). The ratio of CC₅₀ to IC₅₀ was defined as the selectivity index (SI). The compounds of formula (I) were shown to inhibit HIV-1 effectively. Particular IC₅₀, CC₅₀ and SI values are listed in Table 7 hereinbelow. TABLE 7 Co. IC₅₀ CC₅₀ No. (μM) (μM) SI 1 0.027 49.7 1860 2 0.035 >100 >2890 3 0.016 37.4 2558 4 0.315 >100 >317 5 0.094 56.2 598 6 0.020 24.4 1192 7 0.975 >100 >102 8 8.147 >100 >12 9 0.037 58.6 1587 10 2.529 >100 >39 12 1.683 55.1 32 13 0.005 7.8 1557 14 2.183 89.0 40 15 0.003 9.0 2857 16 0.389 41.2 105 17 0.167 9.1 54 18 2.1 59.9 29 19 0.006 53.6 8642 20 0.026 36.5 1413 21 0.017 50.6 2910 22 0.035 12.2 346 23 0.001 47.9 59935 24 0.020 54.0 2667 25 0.079 >100 >1272 26 0.011 33.5 2990 27 0.017 >20 >1169 28 0.079 >20 >253 29 0.015 >20 >1324 30 0.088 >20 >228 31 0.024 86.8 3630 32 0.403 >100 >248 33 0.042 43.4 1038 34 0.319 57.8 181 35 0.103 42.3 409 36 0.323 >100 >309 37 0.443 33.4 75 38 2.449 32.4 13 39 1.531 >100 >65 40 0.253 40.2 158 41 1.986 34.2 17 42 0.352 35.5 88 43 0.603 >100 >165 45 0.010 56.3 5688 46 45.2 >100 >2 47 0.004 >100 >27027 48 44.2 >100 >1 49 0.058 45.2 786 50 0.518 52.0 100 51 0.452 >100 >221 52 0.001 2.08 2314 53 0.0006 1.3 2111 56 0.0023 1.9 839 57 0.0007 0.8 1153 58 0.0029 >100 >34482 59 0.0012 >100 >83333 60 0.29 >100 >350 61 0.0007 0.1 155 62 0.0032 8.7 2716 63 0.0017 0.3 198 64 0.12 >100 >840 65 0.18 0.2 1 66 0.0085 19.9 2347 67 0.0024 0.4 152 68 0.001 1.4 1367 69 0.0004 4.7 11632 70 0.0006 5.8 9641 71 0.0063 45.8 7275 72 0.0007 0.5 705 73 0.0036 >100 >27777 74 0.010 >100 >9523 75 0.0021 1.9 911 76 0.0033 5.2 1580 77 0.0030 9.6 3188 78 0.0028 0.4 144 79 0.0031 4.8 1547 80 0.011 8.7 771 81 0.0011 >100 >90909 82 0.0026 0.4 151 83 0.0008 0.4 541 84 0.012 9.3 753 85 0.002 0.4 208 86 0.010 >100 >9803 87 0.0031 2.2 711 88 0.0027 2.1 767 89 0.0007 0.4 619 90 3.4 30.8 9 91 0.0025 4.9 1976 92 45.0 >90.0 >2 93 0.0035 48.1 13743 94 0.0022 11.1 5064 95 0.0006 7.7 12783 96 0.0031 5.8 1885 97 0.032 13.2 415 98 2.0 13.8 7 99 0.16 59.7 367 100 0.075 0.8 10 101 0.053 29.5 558 102 0.0082 0.5 63 103 0.022 >100 4555 104 0.0034 18.6 5476 105 52.1 <52.1 <1

D. Composition Examples

The following formulations exemplify typical pharmaceutical compositions suitable for systemic administration to animal and human subjects in accordance with the present invention.

“Active ingredient” (A.I.) as used throughout these examples relates to a compound of formula (I) or a pharmaceutically acceptable addition salt thereof.

EXAMPLE D.1

Film-Coated Tablets

Preparation of Tablets Core

A mixture of 100 g of the A.I., 570 g lactose and 200 g starch was mixed well and thereafter humidified with a solution of 5 g sodium dodecyl sulfate and 10 g polyvinyl-pyrrolidone in about 200 ml of water. The wet powder mixture was sieved, dried and sieved again. Then there was added 100 g microcrystalline cellulose and 15 g hydrogenated vegetable oil. The whole was mixed well and compressed into tablets, giving 10,000 tablets, each comprising 10 mg of the active ingredient.

Coating

To a solution of 10 g methyl cellulose in 75 ml of denaturated ethanol there was added a solution of 5 g of ethyl cellulose in 150 ml of dichloromethane. Then there were added 75 ml of dichloromethane and 2.5 ml 1,2,3-propanetriol. 10 g of polyethylene glycol was molten and dissolved in 75 ml of dichloromethane. The latter solution was added to the former and then there were added 2.5 g of magnesium octadecanoate, 5 g of polyvinylpyrrolidone and 30 ml of concentrated color suspension and the whole was homogenated. The tablet cores were coated with the thus obtained mixture in a coating apparatus. 

1.-14. (canceled)
 15. A process for preparing a compound of formula (I′)

a n-oxide, a pharmaceutically acceptable addition salt or a stereochemically isomeric form thereof, wherein L, Q, R³, R⁴, R⁵ and a are as defined under formula (I), and R^(4′) is halo, C₁₋₆alkyl, cyano, aminocarbonyl, nitro, trihalomethyl, trihalomethyloxy or C₁₋₆alkyl substituted with cyano or aminocarbonyl; n′ is 0, 1, 2 or 3; with the proviso that Q and L are other than anilino, 2,4,6-trinitro-anilino, 3-methoxy-anilino, 4-methoxy-anilino, 3,4-dimethoxy-anilino, 3-chloro-4-fluoro-anilino, 4-cyano-anilino, 2-(C₁₋₆alkyl)-anilino, 4-(C₁₋₆alkyl)-anilino, 3-chloro-anilino, 4-bromo-anilino, 4-nitro-anilino and 4-chloro-anilino; wherein the process comprises: a) reacting an intermediate of formula (II-A) wherein W¹ is a suitable leaving group with an amino derivative of formula (III) optionally in a solvent under a reaction-inert atmosphere, and optionally in the presence of an acid

wherein Q, R³, R⁴ ,R^(4′), R⁵, A, n′ and L are as defined as above; b) reacting an intermediate of formula (II-B) wherein W¹ is a suitable leaving group with an amino derivative of formula (VI) optionally in a solvent under a reaction-inert atmosphere, and optionally in the presence of an acid

c) reacting an intermediate H—X¹—R⁶ with an intermediate of formula (II-C) in a suitable solvent optionally in the presence of a suitable acid or base; thus obtaining compounds of formula (I′) wherein L is —X¹—R⁶, said compounds being represented by formula (I′-c).

or if desired, converting compounds of formula (I′) into each other following art-known transformations, and further, if desired, converting the compounds of formula (I′), into a therapeutically active non-toxic acid addition salt by treatment with an acid, or into a therapeutically active non-toxic base addition salt by treatment with a base, or conversely, converting the acid addition salt form into the free base by treatment with alkali, or converting the base addition salt into the free acid by treatment with acid; and, if desired, preparing stereochemically isomeric forms or N-oxides thereof. 17.-24. (canceled) 